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噬菌体T4脱氧核苷酸激酶:基因克隆与酶的纯化

Bacteriophage T4 deoxynucleotide kinase: gene cloning and enzyme purification.

作者信息

Brush G S, Bhatnagar S K, Bessman M J

机构信息

McCollum-Pratt Institute, Johns Hopkins University, Baltimore, Maryland 21218.

出版信息

J Bacteriol. 1990 Jun;172(6):2935-9. doi: 10.1128/jb.172.6.2935-2939.1990.

Abstract

Gene 1 of bacteriophage T4 has been cloned into a lambda pL expression vector, resulting in the overproduction of deoxynucleotide kinase. A procedure that includes affinity chromatography on Cibacron Blue F3GA-agarose has been used to purify milligram quantities of enzymes from a 2-liter culture. The enzyme has been partially characterized in vitro and in vivo, and it appears to be identical to the deoxynucleotide kinase isolated from T4-infected Escherichia coli. These results prove the earlier contention that the phosphorylation of three dissimilar deoxynucleotides (5-hydroxymethyldeoxycytidylate, dTMP, and dGMP), to the exclusion of most others, is catalyzed by a single protein.

摘要

噬菌体T4的基因1已被克隆到λ pL表达载体中,导致脱氧核苷酸激酶过量产生。一种包括在Cibacron Blue F3GA-琼脂糖上进行亲和层析的方法已被用于从2升培养物中纯化出毫克量的酶。该酶已在体外和体内进行了部分特性鉴定,并且它似乎与从感染T4的大肠杆菌中分离出的脱氧核苷酸激酶相同。这些结果证明了早期的论点,即三种不同的脱氧核苷酸(5-羟甲基脱氧胞苷酸、dTMP和dGMP)的磷酸化,排除了大多数其他核苷酸,是由单一蛋白质催化的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d31/209091/b8030ec797d6/jbacter00160-0132-a.jpg

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